Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 26121–26140 of 27,157 recalls
Recalled Item: Dynesys¿ Universal spacer 6-45 Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirus¿ intramedullary nail for tibia Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLS Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿-PT lateral proximal 3 hole tibial plate Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynesys¿ L.I.S. Stabilizing cord Rx Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alloclassic¿ SL-Offset Stem sterile Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wagner SL Revision Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wagner cone Prosthesis Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Head Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30¿ Proximal positioner Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel Recalled by...
The Issue: Eon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Fracture Humeral Head Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul¿ LDH¿ Head Rx Sterile Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox¿ delta Ceramic Femoral Head Rx only Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30 Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Inverse/Reverse Screw system Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Ball taper for humeral stem Recalled by Zimmer, Inc....
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Fracture Humeral stem Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DTO" Implant Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 Recalled by Davol, Inc.,...
The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.